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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol.

(+)-Magnostellin C, which is a tetrahydrofuran type of lignan bearing a chiral secondary benzylic hydroxy group, was stereoselectively synthesized from L-arabinose by using threo selective aldol condensation.[1]

References

  1. First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol. Yamauchi, S., Kinoshita, Y. Biosci. Biotechnol. Biochem. (2001) [Pubmed]
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